Align homocitrate synthase (EC 2.3.3.14) (characterized)
to candidate WP_011766887.1 AZO_RS15865 2-isopropylmalate synthase
Query= BRENDA::D0VY45 (540 letters) >NCBI__GCF_000061505.1:WP_011766887.1 Length = 511 Score = 409 bits (1052), Expect = e-118 Identities = 239/512 (46%), Positives = 328/512 (64%), Gaps = 20/512 (3%) Query: 27 ILDTTLRDGEQSPGAAMTCVQKLETARQLAKLGVDIIEAGFPCASKQDFMAVKMIAEEVG 86 I DTTLRDGEQSPGA+MT +KL ARQL ++ VD+IEAGF AS DF +V+ IAE + Sbjct: 7 IFDTTLRDGEQSPGASMTRDEKLRIARQLERMRVDVIEAGFAAASNGDFESVRSIAEAIK 66 Query: 87 NCVDGNGYVPVITGVSRCNEKDIATAWEALKHAKRPRLRTFIATSPIHMEYKLRKSKDQV 146 + ++R NE DI A EA++ A R R+ TFIATSPIHME KLR + DQV Sbjct: 67 EST--------VCSLARANENDIRRAGEAIRPAARGRIHTFIATSPIHMEKKLRMTPDQV 118 Query: 147 LETARNMVKFARSLGCTDIQFGAEDAARSDKEFLYQIFGEVIKAGATTLTIPDTVGIAMP 206 +E A + +AR DI+F AEDA RS+ +FL +IF VIKAGA T+ +PDTVG +P Sbjct: 119 VEQAVKAIGWAREY-TDDIEFSAEDAGRSEIDFLCRIFDAVIKAGAKTINVPDTVGYNVP 177 Query: 207 FEYGKLIADIKANTPGIENAIMATHCHNDLGLATANTIEGARYGARQLEVTINGIGERAG 266 +Y + + P + I + HCHNDLGLA +N++ GARQ+E TING+GERAG Sbjct: 178 EQYAATLRTLIERVPNADKVIWSVHCHNDLGLAVSNSLAAVMAGARQVECTINGLGERAG 237 Query: 267 NASFEEVVMALTCRGIDILGGLHTGINTRHILKTSKMVEKYSGLHLQPHKALVGANAFLH 326 NAS EE+VMA+ R D+ + T I+T I+ SK+V + +G +QP+KA+VGANAF H Sbjct: 238 NASLEEIVMAVRTRA-DVF-PVSTNIDTTQIVPASKLVSQITGYPVQPNKAIVGANAFAH 295 Query: 327 ESGIHQDGMLKHRGTYEIISPEDIGLVRSVGDTIVLGKLSGRQALRNRLEELGYKL-KDT 385 ESGIHQDG+LKHR TYEI+ ED+G + +VLGK SGR A R RL+ELG ++ + Sbjct: 296 ESGIHQDGVLKHRETYEIMRAEDVGW---GANKLVLGKHSGRNAFRARLQELGIEIGSEE 352 Query: 386 EVEGVFWQFKAVAEKKKRITDTDLRALVSNEAFN-EQPIWKLGDLQVTCGTVGFSTATVK 444 ++ F +FK +A+KK I D DL AL+S+EA EQ ++L + T A V Sbjct: 353 QLNHAFARFKELADKKHEIFDEDLHALMSDEAVTPEQEHFRLVATRFHSETGETPRAEVT 412 Query: 445 LFSIDGSMHVACSIGTGPVDSAYKAINHIVKEPAKLVKYTLGAITEGIDATATTSVEISR 504 L +I G + + G+GPVD+A+KAI + ++L+ Y++ AIT G DA +V +++ Sbjct: 413 L-AIGGQETRSQAEGSGPVDAAFKAIESVAGSGSELLLYSVNAITTGTDAQGEVTVRLAK 471 Query: 505 GDTNHPVFSGTGGGTDVVVSSVDAYLSALNNM 536 + V +G G TD++V+S AYL+ALN + Sbjct: 472 ---DGRVVNGQGADTDIIVASAKAYLNALNKL 500 Lambda K H 0.318 0.134 0.390 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 616 Number of extensions: 26 Number of successful extensions: 8 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 540 Length of database: 511 Length adjustment: 35 Effective length of query: 505 Effective length of database: 476 Effective search space: 240380 Effective search space used: 240380 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory